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Reference type: Journal
Authors: de Barros LA, Pereira LA, Custódio R, Rath S
Article Title: A Novel Computational Approach for Development of Highly Selective Fenitrothion Imprinted Polymer: Theoretical Predictions and Experimental Validations.
Publication date: 2014
Journal: Journal of the Brazilian Chemical Society
Volume: 25
Issue: (4)
Page numbers: 619-628.
DOI: 10.5935/0103-5053.20140009
Alternative URL: http://www.jbcs.sbq.org.br/imagebank/pdf/v25n4a02.pdf

Abstract: The quality of molecularly imprinted recognition sites depend on the mechanisms and the extent of the functional monomer-template interactions present in the prepolymerization mixture. Thus, an understanding of the physical parameters governing these interactions is key for producing a highly selective molecularly imprinted polymer (MIP). In this paper, novel molecular modeling studies were performed to optimize the conditions for the molecular imprinting of fenitrothion. Four possible functional monomers were evaluated. Five porogenic solvents were investigated employing the polarizable continuum method. The MIP based in methacrylic acid (MAA-MIP) synthesized in the presence of toluene shown to be the most thermodynamically stable complex. Contrarily, MIP based in p-vinylbenzoic acid (PVB-MIP) had the lowest binding energy. According to the adsorption parameters fitted by the Langmuir-Freundlich isotherm, MAA-MIP presented twice the number of binding sites compared to PVB-MIP (103.35 and 53.77 μmol g-1, respectively).
Template and target information: fenitrothion
Author keywords: molecularly imprinted polymer, molecular modeling, Gibbs free energy, functional monomer, solvent effect


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